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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2408999Generated: November 4, 2026

Hydrochloric Acid → HCID 86698276, compound

https://huagongshe.com/reaction/2408999

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantSodium HydroxideHCID 14798—
Reactant4-Chloro-6,7-dimethoxyquinazolineHCID 2769364—
ReactantHCID 86698277HCID 86698277—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
ProductHCID 86698276HCID 8669827663.4%

Reaction Steps

To a solution of 4-chloro-6,7-dimethoxyquinazoline (200 mg, 0.89 mmol) in DMF (5 mL) was added sequentially 5-tert-butyl-3-hydroxyselenophene-2-carboxamide (220 mg, 0.89 mmol), powdered NaOH (147 mg, 3.568 mmol) and catalytic amount of KI at rt and the mixture was stirred at rt for 3 h. The mixture was poured into ice cooled water, neutralized with dil. HCl and stirred for 15 min. The precipitated solid was filtered, washed with water and dried. The crude product was chromatographed over silica gel column using chloroform-methanol (95:5) as eluents to give the product as an yellow color solid (245 mg, 63%), mp 220-224° C. 1H NMR (400 MHz, CDCl3): δ 15.16 (1H, br s, exchangeable with D2O), 13.63 (1H, br s, exchangeable with D2O), 8.17 (1H, s), 7.51 (1H, s), 7.21 (1H, s), 6.87 (1H, s), 4.05 (6H, s), 1.38 (9H, s); 13C NMR (100 MHz, CDCl3): δ 175.5, 172.0, 164.8, 156.6. 155.1, 150.7, 145.9, 139.9, 118.7, 113.1, 112.7, 108.4, 103.3, 56.5, 56.3, 37.1, 32.2; LC-MS (positive ion mode): m/z 434, 436 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08815879B2
Source datasetuspto-grants-2014_08
ORD IDord-076f3eb220e74da6a5e2eb20ea8e800c
Source noteuspto-grants-2014_08